Recherche de Sous-structure

818301

CC(=O)NC1(c2ccccc2)CCN(CCOC(CN(C)C(=O)OCc2ccccc2)c2ccc(Cl)c(Cl)c2)CC1.Cl
Reaction #1938
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1(c2ccccc2)CCN(CCOC(CN(C)C(=O)Cc2ccccc2)c2ccc(Cl)c(Cl)c2)CC1.CC(=O)NC1(c2ccccc2)CCN(CCOC(CN(C)C(=O)Cc2ccccc2)c2ccc(Cl)c(Cl)c2)CC1.Cl.Cl.O
Reaction #1939
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #3137
hydrate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1(c2ccccc2)CCN(C(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)CC(CNCc2ccccc2)c2ccc(Cl)c(Cl)c2)CC1
Reaction #3138
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCC(CC(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)N1CCC(NC(C)=O)(c2ccccc2)CC1)c1ccc(Cl)c(Cl)c1
Reaction #3139
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #3140
hemihydrate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #3141
hydrate
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N(C)C1(c2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1.Cl
Reaction #78338
expected product
Rendement 80.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)C1(c2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCCN(C(=O)c3ccccc3)C2)CC1.CN(C)C(=O)C1(c2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCCN(C(=O)c3ccccc3)C2)CC1.Cl.Cl.O
Reaction #78346
expected product
Rendement 80.2%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O.O=C(c1ccccc1)N1CCCCC(CCCN2CCC(C(=O)N3CCCC3)(c3ccccc3)CC2)(c2ccc(Cl)c(Cl)c2)C1.O=C(c1ccccc1)N1CCCCC(CCCN2CCC(C(=O)N3CCCC3)(c3ccccc3)CC2)(c2ccc(Cl)c(Cl)c2)C1
Reaction #78347
expected product
Rendement 32.3%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Nc1nc(C2(c3ccccc3)CCN(CCCC3(c4ccc(Cl)c(Cl)c4)CCCCN(C(=O)c4ccccc4)C3)CC2)cs1
Reaction #78348
3-[3-[4-(2-Aminothiazol-4-yl)-4-phenylpiperid-1-yl]propyl]-1-benzoyl-3-(3,4-dichlorophenyl)perhydroazepine Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O.O=C(NC1(c2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1)c1cccs1
Reaction #78352
expected product
Rendement 101.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1(c2ccccc2)CCN(CCC(c2ccc(Cl)c(Cl)c2)C(OC(C)=O)c2ccnn2-c2ccccc2)CC1
Reaction #178137
DOI: 10.1039/C8SC04228D
CC(=O)NC1(c2ccccc2)CCN(CCCC2CC2(C(=O)N(C)Cc2ccc(F)cc2)c2ccc(Cl)c(Cl)c2)CC1
Reaction #185046
DOI: 10.1039/C8SC04228D
Cc1cc(C(=O)c2cc(N3CCC4(CC3)NC(=O)Nc3ccccc34)ncn2)cc2oc(=O)[nH]c12
Reaction #202022
DOI: 10.1039/C8SC04228D
COc1cc2c(cc1OC)C1(CCN(CCc3ccc([N+](=O)[O-])cc3)CC1)N(Cc1ccc([N+](=O)[O-])cc1)CC2=O
Reaction #202112
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCC(NC(C)=O)(c2ccc(Cl)cc2)C(C)(C)C1
Reaction #208374
DOI: 10.1039/C8SC04228D
CC(=O)NC1(c2ccccc2)CCNCC1
Reaction #208863
DOI: 10.1039/C8SC04228D
O=C1Nc2ccccc2C2(CCN(C(=O)C[C@@H]3Cc4cc(Cl)c5[nH]ncc5c4CN(CC(F)(F)F)C3=O)CC2)N1
Reaction #219687
(S)-4-chloro-7-(2-oxo-2-(2′-oxo-2′,3′-dihydro-1′H-spiro[piperidine-4,4′-quinazoline]-1-yl)ethyl)-9-(2,2,2-trifluoroethyl)-6,7,9,10-tetrahydroazepino[3,4-e]indazol-8(3H)-one
Rendement 79.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cccc(C2(N)CCN(C(=O)OCc3ccccc3)CC2)c1
Reaction #226406
DOI: 10.1039/C8SC04228D
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